Kathrin Thomay

593 total citations
16 papers, 182 citations indexed

About

Kathrin Thomay is a scholar working on Molecular Biology, Hematology and Physiology. According to data from OpenAlex, Kathrin Thomay has authored 16 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Hematology and 4 papers in Physiology. Recurrent topics in Kathrin Thomay's work include Acute Myeloid Leukemia Research (9 papers), Telomeres, Telomerase, and Senescence (4 papers) and Epigenetics and DNA Methylation (3 papers). Kathrin Thomay is often cited by papers focused on Acute Myeloid Leukemia Research (9 papers), Telomeres, Telomerase, and Senescence (4 papers) and Epigenetics and DNA Methylation (3 papers). Kathrin Thomay collaborates with scholars based in Germany, United States and Slovakia. Kathrin Thomay's co-authors include Brigitte Schlegelberger, Gudrun Göhring, Yvonne Lisa Behrens, Winfried Hofmann, Bruce C. Trapnell, Mania Ackermann, Hans Kreipe, Thomas Moritz, Miriam Hetzel and Takuji Suzuki and has published in prestigious journals such as Blood, American Journal of Respiratory and Critical Care Medicine and International Journal of Molecular Sciences.

In The Last Decade

Kathrin Thomay

16 papers receiving 181 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Kathrin Thomay Germany	7	81	65	34	32	32	16	182
Yvonne Lisa Behrens Germany	8	62 0.8×	78 1.2×	34 1.0×	48 1.5×	50 1.6×	21	210
Jacquelyn Myers United States	9	119 1.5×	53 0.8×	11 0.3×	13 0.4×	56 1.8×	15	228
Stuart Hay United States	3	174 2.1×	56 0.9×	12 0.4×	13 0.4×	84 2.6×	3	238
Kristen E. Schratz United States	7	108 1.3×	90 1.4×	152 4.5×	21 0.7×	45 1.4×	10	272
Giorgia Saporiti Italy	8	41 0.5×	55 0.8×	8 0.2×	20 0.6×	51 1.6×	18	177
Orna Steinberg‐Shemer Israel	8	113 1.4×	85 1.3×	61 1.8×	9 0.3×	28 0.9×	30	237
Marissa Rashkovan Canada	6	119 1.5×	107 1.6×	9 0.3×	42 1.3×	55 1.7×	7	210
Antonella Santoro United Kingdom	6	195 2.4×	116 1.8×	14 0.4×	12 0.4×	71 2.2×	10	290
Klas Raaschou‐Jensen Denmark	8	65 0.8×	175 2.7×	17 0.5×	35 1.1×	74 2.3×	22	262
Raphael Teipel Germany	8	59 0.7×	137 2.1×	10 0.3×	19 0.6×	30 0.9×	21	196

Countries citing papers authored by Kathrin Thomay

Since Specialization

Citations

This map shows the geographic impact of Kathrin Thomay's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kathrin Thomay with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kathrin Thomay more than expected).

Fields of papers citing papers by Kathrin Thomay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathrin Thomay. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kathrin Thomay. The network helps show where Kathrin Thomay may publish in the future.

Co-authorship network of co-authors of Kathrin Thomay

This figure shows the co-authorship network connecting the top 25 collaborators of Kathrin Thomay. A scholar is included among the top collaborators of Kathrin Thomay based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kathrin Thomay. Kathrin Thomay is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Thomay, Kathrin, Jana Lentes, Yvonne Lisa Behrens, et al.. (2021). Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing. Genes Chromosomes and Cancer. 61(1). 22–26. 4 indexed citations

Schieck, Maximilian, Jana Lentes, Kathrin Thomay, et al.. (2020). Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia. Annals of Hematology. 99(4). 809–818. 25 indexed citations

Behrens, Yvonne Lisa, Kathrin Thomay, Gunnar Schmidt, et al.. (2019). Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?. Genes Chromosomes and Cancer. 58(3). 139–148. 4 indexed citations

Happle, Christine, Nico Lachmann, Mania Ackermann, et al.. (2018). Pulmonary Transplantation of Human Induced Pluripotent Stem Cell–derived Macrophages Ameliorates Pulmonary Alveolar Proteinosis. American Journal of Respiratory and Critical Care Medicine. 198(3). 350–360. 53 indexed citations

Thomay, Kathrin, Jana Lentes, Britta Skawran, et al.. (2018). Effect of TP53 contact and conformational mutations on cell survival and erythropoiesis of human hematopoietic stem cells in a long term culture model. Oncotarget. 9(52). 29869–29876. 2 indexed citations

Feurstein, Simone, Kathrin Thomay, Winfried Hofmann, et al.. (2018). Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q Deletion. International Journal of Molecular Sciences. 19(10). 3269–3269. 6 indexed citations

Thomay, Kathrin, Winfried Hofmann, Hans Kreipe, et al.. (2017). Telomere shortening, TP53 mutations and deletions in chronic lymphocytic leukemia result in increased chromosomal instability and breakpoint clustering in heterochromatic regions. Annals of Hematology. 96(9). 1493–1500. 13 indexed citations

Behrens, Yvonne Lisa, et al.. (2017). Comparison of different methods for telomere length measurement in whole blood and blood cell subsets: Recommendations for telomere length measurement in hematological diseases. Genes Chromosomes and Cancer. 56(9). 700–708. 22 indexed citations

Thomay, Kathrin, Gudrun Goehring, Marcin W. Włodarski, et al.. (2017). Mutational Spectrum of Fanconi Anemia Associated Myeloid Neoplasms. Klinische Pädiatrie. 229(6). 329–334. 14 indexed citations

10.

Thomay, Kathrin, Andrea Schienke, Hans-Heinrich Kreipe, et al.. (2016). Establishing a murine xenograft-model for long-term analysis of factors inducing chromosomal instability in myelodysplastic syndrome: Pitfalls and successes. Cancer Genetics. 209(6). 258–266. 2 indexed citations

11.

Lentes, Jana, Kathrin Thomay, Dominik T. Schneider, et al.. (2016). Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia. Cytogenetic and Genome Research. 150(3-4). 281–286. 1 indexed citations

12.

Ripperger, Tim, Birgit Burkhardt, Fabian Hauck, et al.. (2016). Clinical Heterogeneity in RUNX1-Associated Familial Myelodysplastic Syndrome - Report of Two Novel Pedigrees with Childhoodleukemia. Blood. 128(22). 5509–5509. 1 indexed citations

13.

Schlegelberger, Brigitte, Hans Kreipe, Ulrich Lehmann, et al.. (2015). A child with Li–Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies. Pediatric Blood & Cancer. 62(8). 1481–1484. 14 indexed citations

14.

Ripperger, Tim, Marcel Tauscher, Kathrin Thomay, et al.. (2013). No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21–21q22. Leukemia Research. 37(6). 721–723. 2 indexed citations

15.

Thomay, Kathrin, Andrea Schienke, Ute Modlich, et al.. (2013). Chromosomal Instability and Telomere Shortening in Long-Term Culture of Hematopoietic Stem Cells: Insights from a Cell Culture Model of RPS14 Haploinsufficiency. Cytogenetic and Genome Research. 142(1). 14–20. 5 indexed citations

16.

Thomay, Kathrin, et al.. (2013). Induction of Chromosomal Instability via Telomere Dysfunction and Epigenetic Alterations in Myeloid Neoplasia. Cancers. 5(3). 857–874. 14 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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